261 Jobs für Clinical Research Operations Manager
Stellenangebote Clinical Research Operations Manager Jobs
Neu Job vor 6 Std. bei Jooble gefunden
Alimentiv
• Hamburg
Führungs-/ Leitungspositionen
Responsible for the
clinical operations of a project within a defined regional/ global level. Provides oversight of project deliverables, assigned Clinical
Research Associate (CRAs) and Investigator sites in accordance with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Monitoring Plan, Protocol, Good Clinical Practice (GCP) , ICH guidelines and local regulations. The COL acts as a primary liaison between the CRAs and the clinical project team. Additional responsibilities include project specific training of CRAs, conducting assessment visits with CRAs, [. .. ] for study-specific questions and issues. Escalates to PM and other functions as appropriate. Support line managers by providing status updates on utilization and performance of CRAs. Liaise with line manager for assigning sites to CRAs following line manager allocation of a CRA resource to the project. Conduct CRA Assessment visits per departmental requirements to assess the performance of the CRA against their monitoring responsibilities. Study Documents and Plans Develop training materials and study tools for sites and CRAs, including monitoring [. .. ]
Neu Job vor 6 Std. bei Jooble gefunden
Hologic
Lead Engineer
• Berlin
Führungs-/ Leitungspositionen
[. .. ] - ---------As a leading innovator in the field of women s health, Hologic helps people lead healthier liveseverywhere, every day. The
Research Development (R D) department is [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the driving force behind our daily operations at Hologic. Our R D teams work with state-of-the-art technology, ensuring that our innovations are designed to deliver exceptional clinical outcomes, enabling earlier and more reliable detection, diagnosis, and treatment of diseases and other health conditions. Join our Breast Skeletal Health R D team in Berlin as a Lead Engineer, where youll lead the technical management of product development from the concept phase to series production, as well as technical [. .. ] practices for R D and, where possible, the broader Hologic R D organization to ensure the highest product quality and efficient project execution. Act as deputy to the formal line manager and represents them in technical and organizational matters in their absence. What We Expect In-depth knowledge of medical device development Understanding of regulatory requirements (MDR; ISO 13485) Strong experience of design controls, verification and validation Experience with risk management processes and usability engineering (ISO 14971) Fundamentals of materials, manufacturing [. .. ]
Job vor 2 Tagen bei Jooble gefunden
NVision Imaging Technologies
• Ulm
Homeoffice möglich
[. .. ] technical documentation and manuals. Conduct customer training sessions on product first-line troubleshooting maintenance. Cross-functional Collaboration: Work closely with R D and engineering teams to provide feedback from [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] field operations, supporting product development and continuous improvement initiatives. Participate in testing and evaluating new products, features, and solutions, offering practical insights based on customer interactions. Inventory Management Quality Assurance: Organize and manage spare parts inventory, ensuring availability for timely service delivery. Ensure all service activities comply with industry regulations, safety standards, [. .. ] providing stability and long-term career growth opportunities Enjoyable work atmosphere with an open-door and open communication mentality contact information Any questions? Please contact: Sandra Schärli Senior Talent Acquisition Manager mail: Please note that, for data privacy reasons, we ll not review applications or CVs sent via email. Unsolicited applications can be submitted here. About us NVision is a quantum biotech startup based in Ulm, Germany, with Tier 1 investors from the USA and Europe. We are just leaving stealth [. .. ] local R D to global commercialization and expansion. We are developing a technology that will enable MRI-based imaging of real-time metabolism in the body, with tremendous potential for research and applications in oncology, cardiology, neurology and more. Our company brings together expertise in physics, chemistry, engineering and medicine, and we are collaborating with scientists and clinicians from top medical and research centers such as Memorial Sloan Kettering in New York, MD Anderson in Texas, Technical University of Munich, Cambridge University in the UK and more. NVision is developing fast, robust and easy-to-use hyperpolarization technology for preclinical and clinical research in our POLARIS product line. Those devices are placed close to an MRI scanner in a research or clinical environment to produce hyperpolarized contrast agents on demand in a fast, fully-automated, multi-step chemical process. Key steps of the process contain fluidic transport across multiple vessels and chemical [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Sr CRA in oncology-Sponsor dedicated-Home Based Germany
• München
Sr CRA in oncology-Sponsor dedicated-Home Based Germany Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique
clinical, medical affairs and commercial [...]
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[...] insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to [. .. ] to more junior level CRAs. Performs training and sign off visits for junior CRA staff, as assigned. May be mentored and assigned lead tasks under supervision of an experienced Clinical Operations Lead (COL) or operational line manager. This could include participation in business development proposals and/or defense meetings. Qualifications: Bachelors degree or RN in a related field or equivalent combination of education, training and experience Knowledge of Good Clinical Practice/ ICH Guidelines and other applicable regulatory requirements Preferably oncology experience Must demonstrate good computer skills and [. .. ] accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. Summary Roles within Clinical Monitoring/ CRA job family are responsible for monitoring during clinical research studies to ensure that the trials are being conducted in accordance with widely accepted clinical practices. This includes conducting on-site and remote monitoring, developing tools, procedures, and processes to ensure quality monitoring. Impact and Contribution Individual contributors with responsibility in a professional or technical discipline or specialty, but may [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Abb Vie
• Ludwigshafen am Rhein
Führungs-/ Leitungspositionen
Work-Life-Balance
[. .. ] your colleagues. Are you passionate about improving global health care? In a challenging work environment that offers opportunities of developing and increasing your own skills? Moving mountains [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] together as Principal Research Scientist I/ II/ Biologics Drug Product Lead (R D) (all genders) (full-time, permanent) The scientific background of the incumbent should include formulation, manufacturing process development, container closure systems, quality risk management and analytical development. Solid experience with various molecule types, working in a global team and strategic as well [. .. ] Drug Product Development topics and will work closely with cross-functional subject matter experts from Discovery, analytical, and device development, Quality Assurance, CMC Regulatory Affairs, parental Product Development Science Technology (Operations) and external partners You represent Biologics Drug Product Development Germany as single point of contact in global Product Development Strategy Teams and are responsible for the formulation, manufacturing process and container closure system development of early-stage biological assets up to clinical phase III. You represent Biologics Drug Product Development Germany in project specific early-stage Development Sciences Core Teams connecting discovery with toxicology, DMPK and drug substance and drug product. You translate expert knowledge and project specifics into efficient and patient centric Drug Product development strategies. For this you establish, align, [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Abb Vie
Product Manager (m/w/d) - Full time
• Ludwigshafen am Rhein
Work-Life-Balance
[. .. ] your colleagues. Are you passionate about improving global health care? In a challenging work environment that offers opportunities of developing and increasing your own skills? Moving mountains [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] together as Principal Research Scientist I/ II/ Biologics Drug Product Lead (R D) (all genders) (full-time, permanent) The scientific background of the incumbent should include formulation, manufacturing process development, container closure systems, quality risk management and analytical development. Solid experience with various molecule types, working in a global team and strategic as well [. .. ] Drug Product Development topics and will work closely with cross-functional subject matter experts from Discovery, analytical, and device development, Quality Assurance, CMC Regulatory Affairs, parental Product Development Science Technology (Operations) and external partners You represent Biologics Drug Product Development Germany as single point of contact in global Product Development Strategy Teams and are responsible for the formulation, manufacturing process and container closure system development of early-stage biological assets up to clinical phase III. You represent Biologics Drug Product Development Germany in project specific early-stage Development Sciences Core Teams connecting discovery with toxicology, DMPK and drug substance and drug product. You translate expert knowledge and project specifics into efficient and patient centric Drug Product development strategies. For this you establish, align, [. .. ]
Job vor 4 Tagen bei Jooble gefunden
Abb Vie
• Ludwigshafen am Rhein
Work-Life-Balance
[. .. ] your colleagues. Are you passionate about improving global health care? In a challenging work environment that offers opportunities of developing and increasing your own skills? Moving mountains [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] together as Principal Research Scientist I/ II/ Biologics Drug Product Lead (R D) (all genders) (full-time, permanent) The scientific background of the incumbent should include formulation, manufacturing process development, container closure systems, quality risk management and analytical development. Solid experience with various molecule types, working in a global team and strategic as well [. .. ] Drug Product Development topics and will work closely with cross-functional subject matter experts from Discovery, analytical, and device development, Quality Assurance, CMC Regulatory Affairs, parental Product Development Science Technology (Operations) and external partners You represent Biologics Drug Product Development Germany as single point of contact in global Product Development Strategy Teams and are responsible for the formulation, manufacturing process and container closure system development of early-stage biological assets up to clinical phase III. You represent Biologics Drug Product Development Germany in project specific early-stage Development Sciences Core Teams connecting discovery with toxicology, DMPK and drug substance and drug product. You translate expert knowledge and project specifics into efficient and patient centric Drug Product development strategies. For this you establish, align, [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Contract Clinical Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Study Specialist (Contract)
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Senior Research Associate
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts [. .. ] required. Supports remote monitoring, if and as applicable. Negotiates investigator/ hospital agreements with stakeholders. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive salary with [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Manages the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas, with appropriate supervision. Ensures quality of data submitted from study sites and assures timely submission of data, [. .. ] with stakeholders. Maintains and completes own expense reports as per local and applicable guidelines. Supports new and innovative processes and technologies to increase the quality, productivity, and efficiency of Clinical Operations and conserve overall departmental operating costs. Qualifications Appropriate life-science or healthcare-related qualification or experience or equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Current knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, understand and [. .. ]
Job vor 9 Tagen bei Jooble gefunden
Airs Medical Inc
Technical Customer Success Manager (Europe)
• Homeoffice
Job Description Summary Join the AIRS Medical team as a Technical Customer Success
Manager for the EMEA region and play a vital role in ensuring healthcare clients successfully integrate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] and maximize the value of Swift MR, our cloud-based MRI reconstruction software. This role involves working directly with healthcare providers to set up and configure Swift MR, establish connections with MRI systems and PACS, and troubleshoot [. .. ] experience from setup to ongoing support. AIRS Medical has been recognized with Frost Sullivan s Technology Innovation Leadership Awards (2023 and 2024) and as the winner of the Facebook AI Research and NYU Langone Health fast MRI Challenges (2019 and 2020) , underscoring our leadership in deep learning and medical imaging AI. As we continue expanding across the U. S. , Europe and globally, AIRS Medical remains committed to advancing AI and robotics innovations that enhance patient care, support healthcare professionals, and [. .. ] managing network and DICOM configurations for smooth interoperability Utilize your expertise in TCP/ IP and DICOM networking to troubleshoot and support seamless data transmission and connectivity Manage Swift MRs cloud-based operations to ensure secure and reliable performance for healthcare facilities Customer Support Troubleshooting (50) Act as the primary technical resource for clients, providing application support and resolving technical issues Provide in-depth troubleshooting for integration or connectivity issues related to Swift MR, including PACS support and MRI-specific configurations Develop and maintain [. .. ] English and German Pro-active team player Preferred Experiences (Nice to Have) 3+ years in a technical or application support role within healthcare IT Experience implementing radiology software in a clinical environment Experience with Linux Fluent in Italian Work Conditions and Environment Work type: Full-time Collaborate with team members and customers around the country and the world Hiring Process Initial Coffee Chat Informal discussion to explore mutual fit. Technical Interview (Hiring Manager) Assessment of technical skills and experience. Interview with [. .. ]
Job vor 11 Tagen bei Jooble gefunden
• München
[. .. ] medical affairs strategy, including pre-launch and launch activities, for the companys products/ pipeline in collaboration with the commercial team and aligned with the global strategy. The Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Science Liaison Manager will lead The field team based in Europe with particular focus on its lead molecule in Cardiometabolism, including HCP engagement, congress planning and medical communications/ education. The role will lead and manage the Medical Science Liaisons in Europe, leading their strategic deployment and supporting all activities. Executes and maintains the [. .. ] resource to internal stakeholders (medical, commercial, field teams and other) , providing medical/ scientific knowledge, training, and support on the companys products Key role medical affairs insight gathering processes and operations including leading on working collaboratively towards innovative solutions for identified issues in Europe Ensures that all interactions and activities adhere to corporate and healthcare compliance guidance in all activities, including those related to scientific interactions with internal and external groups, and responses to unsolicited requests for medical/ scientific information Works [. .. ] laws MD, Pharm D, Ph D (or equivalent) degree Extensive medical affairs experience gained in the biotechnology or pharmaceutical industry Experience of leadership and management of previous MSL teams Knowledge of clinical research design and GCP in the Cardiology area Experience in the successful management of vendors and external teams in a matrix environment Experience with medical support of successfully marketed biotechnology or pharmaceutical products. At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. We also encourage you [. .. ]
Job vor 11 Tagen bei Jooble gefunden
Medical Science Liaison Manager
• München
[. .. ] medical affairs strategy, including pre-launch and launch activities, for the companys products/ pipeline in collaboration with the commercial team and aligned with the global strategy. The Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Science Liaison Manager will lead The field team based in Europe with particular focus on its lead molecule in Cardiometabolism, including HCP engagement, congress planning and medical communications/ education. The role will lead and manage the Medical Science Liaisons in Europe, leading their strategic deployment and supporting all activities. RESPONSIBILITIES Develop and maintain, [. .. ] other) , providing medical/ scientific knowledge, training, and support on the companys products Establishes scientific communication and collaboration with HCPs and academia Key role medical affairs insight gathering processes and operations including leading on working collaboratively towards innovative solutions for identified issues in Europe Ensures that all interactions and activities adhere to corporate and healthcare compliance guidance in all activities, including those related to scientific interactions with internal and external groups, and responses to unsolicited requests for medical/ scientific information Works [. .. ] gained in the biotechnology or pharmaceutical industry Therapeutic area experience in Cardiometabolic and rare disease compatible with current pipeline Experience of leadership and management of previous MSL teams Knowledge of clinical research design and GCP in the Cardiology area Experience in the successful management of vendors and external teams in a matrix environment Demonstrable track record of working cross functionally on strategic planning Experience with medical support of successfully marketed biotechnology or pharmaceutical products. At Syneos Health, we are dedicated to building [. .. ]
Job vor 11 Tagen bei Jooble gefunden
• München
[. .. ] medical affairs strategy, including pre-launch and launch activities, for the companys products/ pipeline in collaboration with the commercial team and aligned with the global strategy. The Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Science Liaison Manager will lead The field team based in Europe with particular focus on its lead molecule in Cardiometabolism, including HCP engagement, congress planning and medical communications/ education. The role will lead and manage the Medical Science Liaisons in Europe, leading their strategic deployment and supporting all activities. Executes and maintains the [. .. ] resource to internal stakeholders (medical, commercial, field teams and other) , providing medical/ scientific knowledge, training, and support on the companys products Key role medical affairs insight gathering processes and operations including leading on working collaboratively towards innovative solutions for identified issues in Europe Ensures that all interactions and activities adhere to corporate and healthcare compliance guidance in all activities, including those related to scientific interactions with internal and external groups, and responses to unsolicited requests for medical/ scientific information Works [. .. ] laws MD, Pharm D, Ph D (or equivalent) degree Extensive medical affairs experience gained in the biotechnology or pharmaceutical industry Experience of leadership and management of previous MSL teams Knowledge of clinical research design and GCP in the Cardiology area Experience in the successful management of vendors and external teams in a matrix environment Experience with medical support of successfully marketed biotechnology or pharmaceutical products. At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. We also encourage you [. .. ]
Job vor 11 Tagen bei Jooble gefunden
Medical Manager (m/w/)
• München
[. .. ] medical affairs strategy, including pre-launch and launch activities, for the companys products/ pipeline in collaboration with the commercial team and aligned with the global strategy. The Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Science Liaison Manager will lead The field team based in Europe with particular focus on its lead molecule in Cardiometabolism, including HCP engagement, congress planning and medical communications/ education. The role will lead and manage the Medical Science Liaisons in Europe, leading their strategic deployment and supporting all activities. Executes and maintains the [. .. ] resource to internal stakeholders (medical, commercial, field teams and other) , providing medical/ scientific knowledge, training, and support on the companys products Key role medical affairs insight gathering processes and operations including leading on working collaboratively towards innovative solutions for identified issues in Europe Ensures that all interactions and activities adhere to corporate and healthcare compliance guidance in all activities, including those related to scientific interactions with internal and external groups, and responses to unsolicited requests for medical/ scientific information Works [. .. ] laws MD, Pharm D, Ph D (or equivalent) degree Extensive medical affairs experience gained in the biotechnology or pharmaceutical industry Experience of leadership and management of previous MSL teams Knowledge of clinical research design and GCP in the Cardiology area Experience in the successful management of vendors and external teams in a matrix environment Experience with medical support of successfully marketed biotechnology or pharmaceutical products. At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. We also encourage you [. .. ]
Job vor 11 Tagen bei Jooble gefunden
• München
[. .. ] medical affairs strategy, including pre-launch and launch activities, for the companys products/ pipeline in collaboration with the commercial team and aligned with the global strategy. The Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Science Liaison Manager will lead The field team based in Europe with particular focus on its lead molecule in Cardiometabolism, including HCP engagement, congress planning and medical communications/ education. The role will lead and manage the Medical Science Liaisons in Europe, leading their strategic deployment and supporting all activities. Executes and maintains the [. .. ] resource to internal stakeholders (medical, commercial, field teams and other) , providing medical/ scientific knowledge, training, and support on the companys products Key role medical affairs insight gathering processes and operations including leading on working collaboratively towards innovative solutions for identified issues in Europe Ensures that all interactions and activities adhere to corporate and healthcare compliance guidance in all activities, including those related to scientific interactions with internal and external groups, and responses to unsolicited requests for medical/ scientific information Works [. .. ] laws MD, Pharm D, Ph D (or equivalent) degree Extensive medical affairs experience gained in the biotechnology or pharmaceutical industry Experience of leadership and management of previous MSL teams Knowledge of clinical research design and GCP in the Cardiology area Experience in the successful management of vendors and external teams in a matrix environment Experience with medical support of successfully marketed biotechnology or pharmaceutical products. At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. We also encourage you [. .. ]
Job vor 11 Tagen bei Jooble gefunden
Medical Science Manager
• München
[. .. ] medical affairs strategy, including pre-launch and launch activities, for the companys products/ pipeline in collaboration with the commercial team and aligned with the global strategy. The Medical [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Science Liaison Manager will lead The field team based in Europe with particular focus on its lead molecule in Cardiometabolism, including HCP engagement, congress planning and medical communications/ education. The role will lead and manage the Medical Science Liaisons in Europe, leading their strategic deployment and supporting all activities. Executes and maintains the [. .. ] resource to internal stakeholders (medical, commercial, field teams and other) , providing medical/ scientific knowledge, training, and support on the companys products Key role medical affairs insight gathering processes and operations including leading on working collaboratively towards innovative solutions for identified issues in Europe Ensures that all interactions and activities adhere to corporate and healthcare compliance guidance in all activities, including those related to scientific interactions with internal and external groups, and responses to unsolicited requests for medical/ scientific information Works [. .. ] laws MD, Pharm D, Ph D (or equivalent) degree Extensive medical affairs experience gained in the biotechnology or pharmaceutical industry Experience of leadership and management of previous MSL teams Knowledge of clinical research design and GCP in the Cardiology area Experience in the successful management of vendors and external teams in a matrix environment Experience with medical support of successfully marketed biotechnology or pharmaceutical products. At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. We also encourage you [. .. ]
Job vor 12 Tagen bei Jooble gefunden
Alcedis GmbH
(Senior) Clinical Research Associate/ Klinischer Monitor/ Site Manager (m/w/d) - homebased (Region Berlin und Umgebung)
• Gießen
Homeoffice möglich Abgeschlossenes Studium
Flexible Arbeitszeiten 30+ Urlaubstage
(Senior)
Clinical Research Associate/ Klinischer Monitor/ Site
Manager (m/w/d) - homebased (Region Berlin und Umgebung) bei Alcedis Gmb H softgarden (Senior) Clinical Research Associate/ Klinischer Monitor/ Site Manager [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (m/w/d) - homebased (Region Berlin und Umgebung) Vollzeit Remote Gießen, Deutschland Mit Berufserfahrung 23.01.26 Als (Senior) Clinical Research Associate/ Klinischer Monitor/ Site Manager (m/w/d) unterstützt du unsere Fachabteilung Clinical Operations beim Überwachen und Sicherstellen von Qualitätsmerkmalen in Studienzentren vor Ort sowie bei der erfolgreichen Planung und Durchführung von Klinischen Arzneimittelprüfungen der Phasen I-IV, nicht-interventionellen Studien sowie Medizinprodukte-Studien. Die Rolle ist skalierbar und kann je nach Erfahrung als Lead CRA mit erweiterten Verantwortlichkeiten oder als CRA ausgestaltet werden. [. .. ]
Job vor 14 Tagen bei Jooble gefunden
Beckman Coulter- Diagnostics
Senior Manager Global Accounts Large Network Groups (f/m/d)
• Mülheim an der Ruhr
Homeoffice möglich
[. .. ] and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement, you help turn ideas into impact innovating at the speed of life. As a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratorys role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to [. .. ] best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. Learn about the Danaher Business System which makes everything possible. As a Global Accounts Manager (fm/d) Home Office based-you will be responsible for cultivating strong relationships with global health systems with the goal of providing global business leadership and management of their accounts. You will build and maintain key relationships, develop, and manage opportunities, monitor deployment projects and engage global resources. You will [. .. ] for executive sponsorships, coordinating executive business reviews, and maintaining customer satisfaction. You will own and maintain all aspects of the business within your partnered Large Network Groups (LNG) including supplier operations on behalf of clients, expanding relationships with global clients and managing customer issues for the company. You will be responsible for teaming with the customers executives and leaders across the account, articulating a clear vision and generating enthusiasm, while impacting all relevant business groups. You will sell at the most [. .. ]
Job am 24.01.2026 bei Jooble gefunden
Dr. Falk Pharma GmbH
Clinical Operations Manager Early Clinical Research (m/w/d)
• Regierungsbezirk Freiburg
Flexible Arbeitszeiten
Als Spezialist in der Verdauungs- und Stoffwechselmedizin und Familienunternehmen mit globaler Vernetzung, setzen wir unseren Fokus auf die Entwicklung und den Vertrieb innovativer Arzneimittel für verschiedene Erkrankungen der Leber, der [...]
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[...] Gallenwege, des Darms und der Speiseröhre, um das Leben von Menschen zu verbessern. Wir glauben daran, dass wir [. .. ]
Job am 24.01.2026 bei Jooble gefunden
TFS Health Science
Operational Strategy and Delivery Lead Internal Medicine and Neuroscience
• Mainz
Führungs-/ Leitungspositionen
TFS Health Science is a leading global mid-size Contract
Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire
clinical development journey. Our expertise includes [...]
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[...] full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Operational Strategy and Delivery Lead Internal Medicine and Neuroscience-home based in UK, Germany, Poland, Netherlands or Denmark. As part of our CDS Internal Medicine and Neuroscience team you will working alongside [. .. ] satisfaction Support the Business and Contracts team in developing competitive flexible costing approaches for the BU projects Lead, review and approve proposals offering high quality content, value driven outcomes, efficient operations and competitive costing Studies Strategy and Delivery Participate in proposal and budget development for new opportunities Participate in and/or lead global process improvement initiatives Act as a key relationship manager for assigned customers Responsible for all the assigned BU projects across the portfolio and actively develop and be seen as the first point of escalation to resolve both project management and client issues Responsible to coordinate and lead creative project solutions, leveraging expertise, operational capabilities and technologies to ensure client [. .. ]
Job am 20.01.2026 bei Jooble gefunden
KBR
Special Operations Physical Therapist (Baumholder, Germany)
• Stuttgart
Title: Special
Operations Physical Therapist (Baumholder, Germany) THIS POSITION OFFERS RELOCATION. Belong. Connect. Grow. with KBR KBR is a company of innovators, thinkers, creators, explorers, volunteers, and dreamers; but [...]
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[...] we all share one goal: to improve the world responsibly and safely. We maintain a highly qualified workforce to help care for service people [. .. ] following services in support of POTFFs HP program for SOF personnel, with the priority on SOF Operators and Direct Combat Support personnel: Provide neuro-musculoskeletal injury care, utilizing approved supplemental clinical privileges including the ordering of images, laboratory tests, pharmaceuticals, dry needling, acupuncture, joint injections and aspirations, and referrals to specialty providers. If directed by HP Program Manager and/or Coordinator, directly supervise the PT Tech, PT Assistant, and/or Certified Athletic Trainer (ATC) within their scope of practice. Participate in periodic meetings with HP and POTFF for reasons such as, but not limited to, reviewing care provided to patients. Identify opportunities for improvement. Serve as an advisor to the HP program Manager and/or Coordinator in matters related to Sports Medicine (SM) , injury prevention, rehabilitation, and relevant human performance research. Serve as an advisor to the HP program Manager and/or Coordinator for administrative matters, purchasing of supplies and equipment, and supplemental fiscal requests. Conduct equipment, product, and literature reviews to ensure the HP program stays current with the provision of care. Provide input for the development and utilization of [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Research Operations Manager pro Jahr?
Als Clinical Research Operations Manager verdient man zwischen EUR 60.000,- bis EUR 90.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Research Operations Manager Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 261 offene Stellenanzeigen für Clinical Research Operations Manager Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Research Operations Manager Jobs?
Aktuell suchen 42 Unternehmen nach Bewerbern für Clinical Research Operations Manager Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Research Operations Manager Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Research Operations Manager Stellenangebote:
- Abb Vie (9 Jobs)
- Alimentiv (7 Jobs)
- Beckman Coulter- Diagnostics (7 Jobs)
- TFS Health Science (6 Jobs)
- NVision Imaging Technologies (5 Jobs)
- Thermo Fisher Scientific (5 Jobs)
In welchen Bundesländern werden die meisten Clinical Research Operations Manager Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Research Operations Manager Jobs werden derzeit in Bayern (38 Jobs), Berlin (30 Jobs) und Baden-Württemberg (18 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Research Operations Manager Jobs?
Clinical Research Operations Manager Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
